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24. [A familial case of chronic progressive external ophthalmoplegia associated with mitochondrial disease]. Patte M; Dalens H; Sole P; Sole M; Clavelou P; Boespflug-Tangy O; Beaufrère AM; Bacin F J Fr Ophtalmol; 2001 Nov; 24(9):961-5. PubMed ID: 11912841 [TBL] [Abstract][Full Text] [Related]
25. [Chronic progressive ocular muscular dystrophy v. Graefe. Chronic progressive external ophthalmoplegia (CPEO). Review of the literature based on 294 cases]. Beckmann R; Schmidt D; Ketelsen UP; Schurmann-Bierl K Med Welt; 1978 Jun; 29(25):1030-5. PubMed ID: 661549 [No Abstract] [Full Text] [Related]
26. [Case of progressive external ophthalmoplegia with hemiatrophia totalis]. Matsunaga M; Shida K Naika; 1971 Oct; 28(4):784-8. PubMed ID: 5130083 [No Abstract] [Full Text] [Related]
27. Pigmentary retinopathy in cases of chronic progressive external ophthalmoplegia. Visual sensory aspects. Koerner F Trans Ophthalmol Soc U K (1962); 1972; 92():251-63. PubMed ID: 4541520 [No Abstract] [Full Text] [Related]
28. Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism. Hudson G; Schaefer AM; Taylor RW; Tiangyou W; Gibson A; Venables G; Griffiths P; Burn DJ; Turnbull DM; Chinnery PF Arch Neurol; 2007 Apr; 64(4):553-7. PubMed ID: 17420318 [TBL] [Abstract][Full Text] [Related]
29. [Clinical and genetic study of a case of congenital ophthalmopathy associated with epilepsy]. Truşcă E; Truşcă E; Vitan D Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1979; 24(1):41-6. PubMed ID: 462048 [No Abstract] [Full Text] [Related]
30. [A case of chronic progressive external ophthalmoplegia associated with familial hypercholesterolemia]. Orimo S; Arai M; Hiyamuta E; Goto Y Rinsho Shinkeigaku; 1992 Jan; 32(1):37-41. PubMed ID: 1628435 [TBL] [Abstract][Full Text] [Related]
32. [Progressive external ophthalmoplegia]. García Castaño J; Rollan Landeras A; Pasquau Liaño F; Miralles P; García Román M; Gilsanz Fernández C An Med Interna; 1990 Nov; 7(11):585-7. PubMed ID: 2103214 [TBL] [Abstract][Full Text] [Related]
33. A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism. Mancuso M; Filosto M; Oh SJ; DiMauro S Arch Neurol; 2004 Nov; 61(11):1777-9. PubMed ID: 15534189 [TBL] [Abstract][Full Text] [Related]
34. [Late cerebellar atrophy with osteo-tendinous areflexia and progressive ophthalmoplegia with dominant autosomal heredity. Long-term study in 6 generations of one family]. Bravaccio F; Del Vecchio M; Paolozzi C; Ghetti B; Tripaldelli B; Amati A; Guazzi GC Acta Neurol (Napoli); 1971; 26(3):361-74. PubMed ID: 5094472 [No Abstract] [Full Text] [Related]